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A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
ISSN
1553-7404
Date Issued
2009-11-16
Author(s)
Averdam, Anne
Petersen, Beatrix
Rosner, Cornelia
Neff, Jennifer
Aujard, Fabienne
Münch, Claudia
Schempp, Werner
Carrington, Mary
Shiina, Takashi
Inoko, Hidetoshi
Knaust, Florian
Coggill, Penny
Sehra, Harminder
Beck, Stephan
Abi-Rached, Laurent
Reinhardt, Richard
DOI
10.1371/journal.pgen.1000688
Abstract
There are two main classes of natural killer (NK) cell receptors in mammals, the killer cell immunoglobulin-like receptors (KIR) and the structurally unrelated killer cell lectin-like receptors (KLR). While KIR represent the most diverse group of NK receptors in all primates studied to date, including humans, apes, and Old and New World monkeys, KLR represent the functional equivalent in rodents. Here, we report a first digression from this rule in lemurs, where the KLR (CD94/NKG2) rather than KIR constitute the most diverse group of NK cell receptors. We demonstrate that natural selection contributed to such diversification in lemurs and particularly targeted KLR residues interacting with the peptide presented by MHC class I ligands. We further show that lemurs lack a strict ortholog or functional equivalent of MHC-E, the ligands of nonpolymorphic KLR in ‘‘higher’’ primates. Our data support the existence of a hitherto unknown system of polymorphic and diverse NK cell receptors in primates and of combinatorial diversity as a novel mechanism to increase NK cell receptor repertoire.
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